ライフサイエンスコーパス: HCl

1 HCl gave amphimedine in 8 steps from tryptamine with an

2 HCl is oxidized to generate Cl2 and protons in the anode

3 HCl was studied experimentally and with density function

4 investigate the detection of Fe(3+) in 0.05M HCl+0.05M KCl solution.

5 ling module after elution with 4 mL of 0.05N HCl.

6 processed under mild conditions (0.04-0.08% HCl, 100 degrees C, 60 min).

7 Higher epsilon were obtained in 0.1% HCl methanol (10,797-31,257 L/(mol x cm)) than in aqueou

8 d in MeOH and diluted with either MeOH (0.1% HCl) or buffers to obtain final concentrations between 5

9 n solution containing 200microL of 6molL(-1) HCl.

10 sonication cycle = 74%), using 0.5 mol L(-1) HCl as the extractant, the limits of quantification were

11 on amplitude of 42%, employing 0.5 mol L(-1) HCl as the extracting solvent.

12 tion in Na(2)CO(3)-NH(4)NO(3), 0.5 mol L(-1) HCl, and Resin extraction.

13 urea in 3%(v/v) HCl and 10 mL of 6 mol L(-1) HCl, respectively.

14 15min; and elution solvent, 2mL of 1molL(-1)HCl.

15 nly exhibits strong acid resistance (pH = 1, HCl) but also remains intact even when immersed in satur

16 ferent dextrinization conditions (0.04-0.10% HCl, 100-120 degrees C, 60-180 min) were determined.

17 ons were determined to be 60 degrees C, 0.1M HCl in methanol and 3h without added epicatechin.

18 (E124) reaches maximum in acidic medium (1M HCl - pH 1).

19 tion is also maximal in an acidic medium (1M HCl - pH 2).

20 143) is absorbed in the wider area of pH (1M HCl - pH 6).

21 DGE.2 H2O, BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were deter

22 E.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were determined in archived biosolid samples collec

23 l + CH(3)OH-HCl](+)) or M + 47 ([M + CHCl(2)-HCl](+)).

24 es of Au/CeO(2)&AC when placed in a C(2)H(2)/HCl stream can also rapidly rejuvenate.

25 losions has high molar CO(2)/SO(2) and SO(2)/HCl ratios, while during the passive degassing these rat

26 Reaction of [Ru(PPh(3))(3)HCl] with LiCH(2)TMS, MgMe(2), and ZnMe(2) proceeds with

27 Interference from inorganic acids (HNO(3), HCl, H(2)SO(4), and HF) was investigated with respect to

28 Compound 30.HCl is water-soluble and easily synthesized and serves a

29 rate from minced skins extracted with pH 2.4 HCl containing 23.6KU/g pepsin was the highest (64.19%).

30 ha-form after 3h in 40% NaOH or 1-3 h in 40% HCl solution, and alpha-chitin obtained from NaOH treatm

31 % v/v ethanol:water, 85:15% v/v ethanol:1.5N HCl, and ethanol).

32 ollected in a 1-mL fraction of 90% EtOH/0.9N HCl after removal of (68)Ge-breakthrough in a washing st

33 composition of a HfO2/Al2O3 gate stack on a HCl wet-cleaned In0.53Ga0.47As substrate by comparing th

34 i target dissolved in HNO(3) to convert to a HCl matrix.

35 pproximately 500 muL) of an ammonium acetate/HCl (pH 4.5) solution suitable for direct radiolabeling.

36 acid hydrolysis using 6 M hydrochloric acid (HCl), followed by amino acids derivatization using N,O-b

37 solvents or concentrated hydrochloric acid (HCl).

38 h then combine to produce hydrochloric acid (HCl).

39 r caustic soda (NaOH) and hydrochloric acid (HCl).

40 chloride (FeCl3, 1 M) and hydrochloric acid (HCl, 3 M) and continuously drawing the newly released gr

41 ) extract was examined in the strong acidic (HCl+H2SO4) solution.

42 uminum from primary sludge by acidification (HCl or H2SO4), followed by separation using centrifugati

43 mplest CI, CH2 OO, with two inorganic acids, HCl and HNO3 , both of which are present in polluted urb

44 ine atoms with butenes, that the Cl addition-HCl elimination pathway occurs from an abstraction-like

45 Poly (9-(2-diallylaminoethyl)adenine HCl-co-sulfur dioxide) (Poly A) deposited on silica nano

46 onalized with the polycation poly(allylamine HCl) in a manner that depends on the NOM-to-DNP concentr

47 Two catalysts, an amine HCl salt and a bisthiourea, work in concert to enable th

48 d targets were digested using NH(4)HF(2) and HCl in a closed perfluoroalkoxy alkane vessel in 90 min.

49 The combined use of trifluoroacetic acid and HCl during the synthesis results in a highly crystalline

50 or acidic stimuli, including citric acid and HCl.

51 and N-alkyl nitroanilines using Zn-AcOH and HCl/MeOH, respectively.

52 the presence of carbonyl groups, CF3COOH and HCl for basic sites of different strength, and O3 and NO

53 d DNA (dsDNA) with acetone, ethanol, H2S and HCl.

54 g(HSO4)2 salt solutions as well as H2SO4 and HCl acid solutions are investigated by means of vibratio

55 and in the literature dilute acids, HNO3 and HCl, showed the highest extracted iAs wheras dilute NaOH

56 Microwave power, methanol and HCl concentration significantly (p<0.05) affect extracti

57 es, cyclization, halogen atom migration, and HCl (HBr) elimination.

58 he impact of membrane cleaning with NaOH and HCl on the characteristics and associated changes in ion

59 ation of desalination brine through NaOH and HCl recovery.

60 ses only a common base and an acid, NaOH and HCl to initiate and stop the polymerization reaction, re

61 d that the minor constituents (SO2, NOx, and HCl) significantly modify the percentages of Hg(2+) in t

62 -P pool was bioavailable, whereas NaOH-P and HCl-P pools were recalcitrant during P transport along t

63 se a MtBE-H2O (1:1) system with 10mM TEA and HCl was applied leading to a phenolic fraction, free of

64 ve solid, prepared by treatment of anhydrous HCl with [Et3 SiHSiEt3 ][CHB11 F11 ].

65 lateral turns after injection of apomorphine HCl (p<0.05).

66 s by extraction into toluene from an aqueous HCl solution; unlike current processes, reverse phase tr

67 een carried out in universal buffer, aqueous HCl, and artificial seawater media.

68 ocarbamates with Tin(II) chloride in aqueous HCl.

69 ough topochemical deintercalation in aqueous HCl.

70 study for adduct hydrolysis in 0.1 M aqueous HCl determined that (Fur)dG was the most acid-sensitive

71 nobenzidine and catalytic amounts of aqueous HCl.

72 ) which is about 50-55 % of state-of-the-art HCl electrolysis processes.

73 The optimum conditions were determined as HCl concentration between 0.41 and 0.44mol/L, methanol v

74 of Et4N[H3(BAr(F)3)2], strong acids such as HCl induce H2 release to give the chloride Et4N[(CO)(CNB

75 r derivatives (BADGE.2 H2O, BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.

76 BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were determined in ar

77 products, in addition to propenes, are base.HCl and olefin-bound, cyclometalated dimers [RuCl(kappa(

78 s (prednisolone acetate [generic], betaxolol HCl [Betoptic; Alcon Laboratories Inc., Fort Worth, TX],

79 d and selective Markovnikov addition of both HCl and HBr across several alkene classes under mild rea

80 The DPI-BP/HCl adduct possesses a more planar configuration than DP

81 ) into the solution to dissociate the DPI-BP/HCl adduct.

82 group of DPI-BP to convert it into a DPI-BP/HCl adduct.

83 y HPLC-DAD) and proanthocyanidins (n-butanol/HCl assay), reducing capacity (ferric ion reducing antio

84 cyanidins by depolymerisation with n-butanol/HCl, flavonols by HPLC-DAD, reducing capacity by ferric

85 ur methods of tannin quantification: butanol/HCl, vanillin/HCl, BSA/FeCl(3) and PVPP/Folin-Ciocalteu.

86 The results obtained with butanol/HCl and vanillin/HCl were higher than with BSA/FeCl(3) a

87 m Ajka, Hungary is neutralized to < pH 10 by HCl, gypsum, or seawater addition.

88 troscopic (UV-visible) investigations and by HCl-augmented computational modeling.

89 4-dehydro benzophenanthridine derivatives by HCl hydrolysis.

90 onate and sodium glutarate salts resulted by HCl evaporation from dehydrating particles.

91 found to be affected in aqueous solutions by HCl, NaCl, KCl, and CaCl2 and in acetonitrile by CF3COOH

92 ethyl-3-(3-dimethylaminopropyl) carbodiimide HCl (EDC) has recently been investigated for its effecti

93 Internal stress in bent CFZ-HCl led to photoelastic effects on the azimuthal orienta

94 ocrystals-the hydrochloride salt of CFZ (CFZ-HCl)-has a corrugated packing along the (001) face and w

95 hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation.

96 , at the 2sigma level, in hydrogen chloride (HCl), the main stratospheric chlorine reservoir, startin

97 as well as the bioactive compound Cinacalcet HCl.

98 using data from the Evaluation of Cinacalcet HCl Therapy to Lower Cardiovascular Events trial, a plac

99 s vortex period, and 200 uL of concentrated HCl for 30 mL of sample/standard solution.

100 beo-lupane epoxides under acidic conditions (HCl, montmorillonite K10, and BF(3).Et(2)O) were studied

101 antly up to 20-fold compared to conventional HCl mediated extraction, depending on the mushroom speci

102 yzed cleavage of the resulting cyclopropane (HCl), further improvements in a unique intramolecular cy

103 Enriched phenylalanine, cysteine-HCl and high lysine:arginine ratio could also have benef

104 e was optimized by a 3(2) factorial design (%HCl in methanol, temperature, and time) and response sur

105 Diltiazem-HCl arrested diastolic dysfunction progression in R92W a

106 ion in vivo or by treatment with cold dilute HCl or with excess borate in vitro) enhanced the GIPCs'

107 nt has been developed that allows for dilute HCl (0.05N) to efficiently elute metal-impurity-free (68

108 pensive and nontoxic reagents (NaCl, diluted HCl, water).

109 )-2-(2-quinolin-2-yl-vinyl)-benzene-1,4-diol HCl) hereafter designated Q8.

110 Direct HCl solution calorimetric measurements show the compound

111 iminates the need to buy new Cl2 and dispose HCl waste.

112 ynergistic effect of the combination of DMAP/HCl/Schreiner's thiourea in catalyzing dehydrative glyco

113 recovery from the sympathomimetic dobutamine HCl, one day after exposure.

114 stained low rates (0.15 mug / hr) of (R)-DOI.HCl to mice fed a high-fat "Western" diet.

115 ent with either gaseous water or gaseous dry HCl.

116 ciently promoted by catalytic amounts of dry HCl.

117 DCC and the subsequent elimination of either HCl or MeCl, with ~0.58 equiv of HCl released per mechan

118 plex and the beneficial effect of added Et3N.HCl on yield and enantioselectivity is elucidated: chlor

119 extracts containing it, diluted with ethanol-HCl to assess total flavonoids and anthocyanins in the s

120 HCl (100:1, v/v) (W2), ethanol (E3), ethanol:HCl (100:1, v/v) (E4), dichloromethane (D5) and hexane (

121 of cation-exchange chromatography using EtOH/HCl medium has been developed.

122 ichloroethene (DCE), due to competition from HCl formation.

123 OH)2 addition which limited pH declines from HCl, volatile fatty acids (VFAs), and inorganic carbon (

124 losing the photocycle for H2 generation from HCl.

125 Onsite Cl2 regeneration from HCl is highly desirable as it eliminates the need to buy

126 Gaseous HCl as a by-product is often produced from chlorination

127 A gaseous HCl electrolysis with Fe(3+) /Fe(2+) redox-mediated cath

128 ic chlorine in the presence of H2 to gaseous HCl, was coupled to a dual-detection system, combining a

129 as well as being a source of halogen gases (HCl, ClNO2, etc.).

130 kdown of Atg9a or treatment with gemcitabine HCl resulted in enhanced stimulator of IFN genes-mediate

131 The reaction utilizes in situ generated HCl as the source of both the Cl(-) and H(+) and is cata

132 olished by the denaturants triton X-100, Gua-HCl, Gua-thiocyanate, SDS and urea in a dose-dependent m

133 of the alpha2 adrenergic agonist, guanfacine HCl, on responses to stress and drug cue in a group of c

134 ich were measured independently by guanidine HCl-induced unfolding titrations using purified proteins

135 nt, and chaotropic reagents (urea, guanidine HCl) by monitoring the yield of released desulfurated DM

136 H2O, CO2, SO2, O2, H2, H2S, HCl, chlorinated hydrocarbons, NO, and other trace gases

137 ion bias due to formation of byproducts HCN, HCl, and H2S.

138 r is produced by placing the carbides in HF, HCl or NaCl solutions and applying anodic potentials.

139 , for other variables, such as solvent (HNO3:HCl), final concentration (1.7molL(-1)) and time (26min)

140 the species present in the crystal, 5Me-HQE.HCl, was lost HCl upon sublimation but did not tautomeri

141 transfer between O2 and liquid hydrocarbons, HCl dissociation in salty water, and super-Maxwellian he

142 e structure sensitive reaction to illustrate HCl surface structure effects.

143 t on polyaniline film using Fe(2+)/Fe(3+) in HCl as the redox system shows five distinct linear segme

144 hese challenges and characterize actinium in HCl solutions using X-ray absorption spectroscopy and mo

145 of Au obtained by anodic stripping of Au in HCl solution was used to evaluate the average diameter o

146 tammetry of AuNPs after their dissolution in HCl.

147 We find that p-type doping in HCl/H(2)O atmosphere is related to the rearrangement of

148 y comparisons between Ac(III) and Am(III) in HCl solutions indicate Ac(III) coordinates more inner-sp

149 It can be strongly suppressed in HCl medium by partial hydrolysis of THB with optimal con

150 BAB), and sodium tetrahydridoborate (THB) in HCl and HClO4 media, in the presence or absence of L-cys

151 The parent reagent and its HCl salt present stability and detonation risks, but the

152 5mL of 1mol/L HCl was used as eluent.

153 1 mL of 1 mol/L HCl and 5% thiourea was used as eluent.

154 structures by digestion with boiling 6 mol/L HCl.

155 For the latter, common reagents like HCl, Na2CO3, glycine buffer, or SDS are employed.

156 resent in the crystal, 5Me-HQE.HCl, was lost HCl upon sublimation but did not tautomerize.

157 6-dicarboxylic acid hydrochloride (LY3020371.HCl, 19f), a potent, selective, and maximally efficaciou

158 H (pH: 13.4) was added to 3.7 muL of 0.058 M HCl (pH: 1.24).

159 Im chi((2)) spectra of 1.1 M H2SO4 and 1.1 M HCl acid solutions indicate that HSO4(-) ions have a sim

160 different oxidation states (prepared in 1 M HCl and 1 M HClO(4)) have been determined by capillary e

161 e sensor is regenerable by treating with 1 M HCl and can be used for multiple analysis with little re

162 e of calcium-bound P (Ca-P, extracted by 1 M HCl) due to (1) P redistribution during the alkaline ext

163 procedures for polonium samples (0.1 to 1 M HCl).

164 optimized (0.05 mg of Cu(2+) in 10 mL of 1 M HCl); these compare advantageously with conventional pre

165 f poorly crystalline Fe and Al oxides by 1 M HCl, releasing P occluded by these oxides into solution.

166 h 1.1 M H2SO4 being more enhanced than 1.1 M HCl.

167 ctivity and durability are achieved in 0.1 m HCl.

168 y inert in very harsh conditions such as 2 M HCl, with no dissociation being observed for at least 5

169 arsh environments, such as strong acids (3 m HCl or 3 m H(2) SO(4) for one week), a strong base (20 m

170 A loss of ca. 50% of 0.5 M HCl-extractable Fe(II) [5-10 mmol Fe(II) L(-1)] and dete

171 To do this, we administered MDMA-HCl (100 mg p.o.) and, separately, placebo (ascorbic aci

172 olar nucleophilic methanol alone or methanol-HCl extracts.

173 ined by the incorporation of a >30 per mille HCl vapor from a highly evolved LMO.

174 Minocycline HCl 1 mg microspheres were applied on biofilms on days 2

175 er dimer and trimer, HCl clusters, and mixed HCl-water clusters are the major topics, but related wor

176 rophenyl octyl ether (NPOE) as SLM and 10 mM HCl as sample/acceptor solutions.

177 cumene; donor, 1 muL of basic drugs in 10 mM HCl; and extraction potential, 250 V), experimentally de

178 lvent (D2O) KIEs are (D2O)k = 0.20 in 200 mM HCl, (D2O)k = 0.81 in 50 mM HCl, and (D2O)k = 4.2 in pur

179 mu-EME conditions (acceptor, 1 muL of 25 mM HCl; FLM, 1 muL of 4-nitrocumene; donor, 1 muL of basic

180 = 0.20 in 200 mM HCl, (D2O)k = 0.81 in 50 mM HCl, and (D2O)k = 4.2 in pure water.

181 ater, and the (63)Zn was eluted using 0.05 N HCl in 90% acetone.

182 timonate (BAHA, 1.1 equiv) in aqueous 0.05 N HCl/trifluoroethanol (1-10:1) at room temperature (25 de

183 TX-OCT-Alg had a negligible release in 0.1 N HCl, while the CTX-OCT was completely released after 300

184 n freely moving rats to examine how naloxone-HCl and naloxone-methiodide, the latter which is commonl

185 to be ~40-fold less permeable than naloxone-HCl across the blood-brain barrier, thus acting as a sel

186 Similar to naloxone-HCl, naloxone-methiodide at a relatively low dose (2 mg/

187 ild heating react via elimination of neutral HCl.

188 have similar concentrations of SO2, NO, NO2, HCl, and H2O, the proportion of Hg(0)/Hg(2+) is similar

189 surements to be derived from the activity of HCl reported by the sensor system over the range of ocea

190 The reactions occur through 1,3-addition of HCl across a B-C bond of the NHC-borirane to form a ring

191 1 transformation involves formal addition of HCl across the Mo horizontal lineN imido bond through in

192 experimental selectivity in the addition of HCl to 1,3-pentadiene.

193 The oxidative addition of HCl to 2 selectively yields the cis-hydride-alkylidyne c

194 Stoichiometric addition of HCl to the Co(I)-(N2) cleanly affords the Co(III) hydrid

195 ling that it undergoes oxidative addition of HCl, CH(3)I, and PhI, accompanied by an unusual migratio

196 otoredox catalyst system for the addition of HCl, HF and also phosphoric and sulfonic acids to alkene

197 In contrast, with a small amount of HCl, all of the newly formed Pd(2+) ions could be quickl

198 ent to continuously release small amounts of HCl by thermolytic elimination.

199 ontrol is determined by the concentration of HCl in the water phase of the microemulsion.

200 The optimal concentration of HCl was 2 mol L(-1); the optimal concentration of NaBH4

201 ediment containing a higher concentration of HCl-extractable Fe(II).

202 With high concentrations of HCl (e.g., 1.2-1.5 M), all aggregates break up and the k

203 Additionally, using high concentrations of HCl further reduces the production of the less volatile

204 med not only that very low concentrations of HCl generated from the solvent were responsible for the

205 stric conditions with high concentrations of HCl.

206 Subsequent base-induced beta-elimination of HCl proceeds selectively to give nitrobenzylic alpha-flu

207 2) g(-1), respectively, only when 2 equiv of HCl (0.22 M) was used.

208 n of either HCl or MeCl, with ~0.58 equiv of HCl released per mechanophore activation and ~67 protons

209 The generation of HCl at room temperature from a mixture of sodium chlorid

210 neamino)-benzonitrile (1) in the presence of HCl to produce 2-chloro-3-phenyl-4(3H)-quinazoliniminium

211 Release of HCl from this salt can be manifested in chlorination and

212 (rac-BINAP) was detected from the release of HCl in the dehydrogenation and subsequent reaction with

213 -dibromophenol as a stoichiometric source of HCl to facilitate catalyst turnover.

214 work represents the first successful use of HCl, the simplest strong Bronsted acid, as an efficient

215 med at either M + 45 ([M + CH(2)Cl + CH(3)OH-HCl](+)) or M + 47 ([M + CHCl(2)-HCl](+)).

216 odies and (2) reducing the volume of NH(2)OH.HCl solution can effectively shorten the overall isolati

217 od involves slow addition of aqueous NH(2)OH.HCl to the Bi target dissolved in HNO(3) to convert to a

218 ptimized because (1) the quantity of NH(2)OH.HCl used appears to affect the radiolabeling yield of ph

219 The amount of NH(2)OH.HCl was optimized because (1) the quantity of NH(2)OH.HC

220 ported by systematic investigations based on HCl titration and dynamic light scattering measurements.

221 )) with 100% efficiency with the use of only HCl and NaBH4 as the reagents.

222 results reported here show that the optimal HCl percentage in the water phase is about 25% to obtain

223 ons such as trifluoroacetic acid (10-20%) or HCl (0.1-4.0 N) at room temperature, and the formation o

224 n or concentration of the parent compound or HCl salt and will facilitate the use of hydrogen sulfate

225 on of sources of H(+)/e(-) (H(2), TEMPO-H or HCl), (P(6)ArC)Fe(2)(mu-H) is activated toward N(2) bind

226 urn to the outward-facing state in a KCl- or HCl-bound form.

227 y in strong acid or base (e.g., 12 m NaOH or HCl) and boiling water.

228 rivatives were obtained by saponification or HCl acidolysis of o-boronato-phosphonium amino esters, r

229 arison with the CH method, the pepsin-HCl (P-HCl) method is simpler, avoiding solvent evaporation, di

230 )-enantiomer over the ( S)-enantiomer of PEA-HCl.

231 In comparison with the CH method, the pepsin-HCl (P-HCl) method is simpler, avoiding solvent evaporat

232 e within the NU-1000 pores via a vapor-phase HCl treatment, a silica layer is created on the inner wa

233 ignin content was measured by phloroglucinol-HCl staining, and acetyl bromide and thioacidolysis meth

234 Photodriven HCl splitting to produce solar fuels is an important goa

235 reaction of pioglitazone hydrochloride (PIO-HCl) at a very low drug loading (1% w/w).

236 tween NH(3) and the Cl ligands that produces HCl.

237 Propranolol HCl, as well as very small sugar particles from the pell

238 starter cores were layered with propranolol HCl and subsequently coated with Kollicoat SR, plasticiz

239 x10(-4)molkg(-1) thiamine HCl and pyridoxine HCl solutions.

240 35)molkg(-1) thiamine HCl(aq) and pyridoxine HCl(aq) solutions over temperature range (288.15-318.15)

241 l-ascorbic acid, thiamine HCl and pyridoxine HCl.

242 protic state and the Cl(-) together resemble HCl as the weak coordination.

243 ling that the compounds function as 'strict' HCl cotransporters.

244 The HCl promoted 1,4-elimination of water, whereas in the pr

245 (The HCl-exchanged QBs are insufficiently stable for elementa

246 The minerals were stable and the HCl extractability decreased in the ozonated samples.

247 The important autocatalytic effect of the HCl reaction product was confirmed by spectroscopic (UV-

248 The applicability of the HCl/HFIP method is illustrated by the synthesis of a sul

249 carried out in 1.0x10(-4)molkg(-1) thiamine HCl and pyridoxine HCl solutions.

250 0.05, 0.15, 0.25 and 0.35)molkg(-1) thiamine HCl(aq) and pyridoxine HCl(aq) solutions over temperatur

251 eported earlier in l-ascorbic acid, thiamine HCl and pyridoxine HCl.

252 ow how the exposure of plant-based fibers to HCl vapor results in rapid degradation with simultaneous

253 arger relative conversion of source gases to HCl.

254 tected monosaccharides that are subjected to HCl/HFIP treatment.

255 cohols, which are normally unreactive toward HCl catalysis.

256 VP of the water dimer and trimer, HCl clusters, and mixed HCl-water clusters are the major

257 as achieved with crude extract at pH 7, Tris-HCl binding buffer at pH 7 and the use of 300 mM imidazo

258 Phosphate and Tris-HCl buffers decrease the signal intensity measured in Fe

259 ons of ionic strength (163 mM) in 50 mM Tris-HCl (pH 7.4) at 37 degrees C.

260 ssium glutamate and 8 mM MgCl2 or 10 mM Tris-HCl and 200 mM KCl, with or without 0.5% Tween added to

261 ed directly from a 150 mM KCl and 25 mM Tris-HCl buffer at pH 7 that is widely used in protein chemis

262 ysis buffer with high concentrations of Tris-HCl and sodium dodecyl sulfate as well as exposure to hi

263 On the other hand, the use of Tris-HCl as binding buffer gave higher purification performan

264 ction buffers (phosphate buffer saline, Tris-HCl and NaCl) on the extraction efficiency of total prot

265 s higher using 0.5M NaCl as compared to Tris-HCl and phosphate buffer saline.

266 An extraction procedure using Tris-HCl buffer solution was employed in order to extract wat

267 The extract obtained using Tris-HCl/DDT buffer (pH 8) was used in the pre-treatment of f

268 -46.5%) bound to the column eluted with Tris-HCl buffer, pH 7.5 with a yield up to 76.6%.

269 ) and Cetylpyridinium chloride (CPC) in Tris/HCl buffer, pH 8.5.

270 h and 121 degrees C/30 min, at pH 1-7 using HCl, formic or citric acid as acidulants.

271 to compare the effects of pH adjusted using HCl vs CO2.

272 ) and acid-soluble ash (ASA) fractions using HCl.

273 ve assisted extraction was carried out using HCl 1molL(-1) in order to maintain the integrity of the

274 hat reported for germanane synthesized using HCl, which is promising for incorporation of GeH in sola

275 rbal powder, 0.1% m/v citric acid and 2% v/v HCl was injected into the VG-ICP-MS system for the deter

276 using 10 mL of 0.1%(m/v) thiourea in 3%(v/v) HCl and 10 mL of 6 mol L(-1) HCl, respectively.

277 ethods of tannin quantification and vanillin/HCl stood out for its high accuracy degree.

278 sults obtained with butanol/HCl and vanillin/HCl were higher than with BSA/FeCl(3) and PVPP/Folin-Cio

279 tannin quantification: butanol/HCl, vanillin/HCl, BSA/FeCl(3) and PVPP/Folin-Ciocalteu.

280 s of these bio-residues in water (W1), water:HCl (100:1, v/v) (W2), ethanol (E3), ethanol:HCl (100:1,

281 res based on subtle pKa differences, whereas HCl addition leads to a rapid formation of mixed compone

282 (P)N(H))] is generated by reaction of 3 with HCl or by direct photolysis of 2 in chlorobenzene.

283 Si:L (L: = C{N(2,6-(i)Pr2C6H3)CH}2) (8) with HCl.NC5H5 results in carbene-stabilized Si2Cl2 (2) and s

284 ted carboxylates, a sample is acidified with HCl, and the quantity of H(+) absorbed is determined fro

285 how fluorescence quenching upon binding with HCl likely due to the smaller pi-conjugation structure,

286 c acid for total As and Sb, and boiling with HCl for total Se.

287 On the other hand, cleaning with HCl had a negligible impact on the zeta potential and pe

288 nocatalyst that operates in combination with HCl.

289 Cu and CA could be recovered completely with HCl.

290 ts revealed that TLSB could be desorbed with HCl to recover Zn(II) and Cd(II) and with HNO(3) to reco

291 The treatment of dihydrobetulin with HCl or K10 produced abeo-lupane olefins.

292 htforward removal of the sulfinyl group with HCl yields the highly enantiomerically enriched amine hy

293 d Sb(III) ions were removed by leaching with HCl (50%v/v) and the polymer was characterised by FT-IR

294 fast; at 295 K, the reactions of CH2 OO with HCl and HNO3 have rate constants of 4.6x10(-11) cm(3) s(

295 ester substituents on the borirane ring with HCl provides stable gamma-NHC-bora-gamma-lactones in iso

296 )O was found during the reaction of THB with HCl, H2SO4, and HClO4, while HG from CH3COOH or TRIS buf

297 recapitulated in vitro with treatments with HCl, pepsin, or sarkosyl.

298 BP and is expected to bind the same way with HCl.

299 by the simple reaction of metallic zinc with HCl in water for H2 and DCl in deuterated water for D2.

300 rder were randomized to placebo or yohimbine HCl (10.8 mg) 1 hour before each of four exposure sessio